Advertisement Janssen wins clearance for premature ejaculation drug in Finland and Sweden - Pharmaceutical Business review
Pharmaceutical Business review is using cookies

ContinueLearn More
Close

Janssen wins clearance for premature ejaculation drug in Finland and Sweden

Janssen-Cilag EMEA, a division of Janssen Pharmaceutica, has announced that Priligy has received marketing authorization in Finland and Sweden for the on-demand treatment of premature ejaculation in men 18-64 years of age.

The initial products will be directed to the ovarian cancer biomarker, HE4, which is FDA-cleared for monitoring the progression or recurrence of epithelial ovarian cancer. Fujirebio also grants BD, through its BD Diagnostics – TriPath platform, access to its other cancer biomarkers for inclusion in future multiplex diagnostic products.

“BD is investing in the development of tools and technologies essential for biomarker-guided cancer care. We believe that biomarker testing in a multiplex format can provide clinicians with a powerful toolset for detecting cancer at an earlier stage, which could allow them to begin treatment sooner and improve outcomes,” said Wayne Brinster, Vice President and General Manager for Women’s Health and Cancer, BD. “By incorporating Fujirebio Diagnostics’ cancer biomarkers within our own cancer diagnostics development program, we believe that we are poised to provide clinicians with innovative diagnostic tools for improved patient management and contribute to BD’s growth in cancer diagnostics.”

“This alliance with BD is an excellent strategic fit for Fujirebio Diagnostics’ business,” said Paul Touhey, president and chief executive officer, Fujirebio. “It will increase the use of HE4 as a tool in monitoring ovarian cancer and allow Fujirebio Diagnostics to utilize its expertise in cancer biomarker development and manufacturing, providing to physicians additional tools to manage cancer patients.”